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A Nonenzymatic Analog of Pyrimidine Nucleobase Biosynthesis
Metabolic theories for the origin of life posit that inorganic catalysts enabled self‐organized chemical precursors to the pathways of metabolism, including those that make genetic molecules. Recently, experiments showing nonenzymatic versions of a number of core metabolic pathways have started to s...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9325535/ https://www.ncbi.nlm.nih.gov/pubmed/35304939 http://dx.doi.org/10.1002/anie.202117211 |
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author | Yi, Jing Kaur, Harpreet Kazöne, Wahnyalo Rauscher, Sophia A. Gravillier, Louis‐Albin Muchowska, Kamila B. Moran, Joseph |
author_facet | Yi, Jing Kaur, Harpreet Kazöne, Wahnyalo Rauscher, Sophia A. Gravillier, Louis‐Albin Muchowska, Kamila B. Moran, Joseph |
author_sort | Yi, Jing |
collection | PubMed |
description | Metabolic theories for the origin of life posit that inorganic catalysts enabled self‐organized chemical precursors to the pathways of metabolism, including those that make genetic molecules. Recently, experiments showing nonenzymatic versions of a number of core metabolic pathways have started to support this idea. However, experimental demonstrations of nonenzymatic reaction sequences along the de novo ribonucleotide biosynthesis pathways are limited. Here we show that all three reactions of pyrimidine nucleobase biosynthesis that convert aspartate to orotate proceed at 60 °C without photochemistry under aqueous conditions in the presence of metals such as Cu(2+) and Mn(4+). Combining reactions into one‐pot variants is also possible. Life may not have invented pyrimidine nucleobase biosynthesis from scratch, but simply refined existing nonenzymatic reaction channels. This work is a first step towards uniting metabolic theories of life's origin with those centered around genetic molecules. |
format | Online Article Text |
id | pubmed-9325535 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93255352022-07-30 A Nonenzymatic Analog of Pyrimidine Nucleobase Biosynthesis Yi, Jing Kaur, Harpreet Kazöne, Wahnyalo Rauscher, Sophia A. Gravillier, Louis‐Albin Muchowska, Kamila B. Moran, Joseph Angew Chem Int Ed Engl Communications Metabolic theories for the origin of life posit that inorganic catalysts enabled self‐organized chemical precursors to the pathways of metabolism, including those that make genetic molecules. Recently, experiments showing nonenzymatic versions of a number of core metabolic pathways have started to support this idea. However, experimental demonstrations of nonenzymatic reaction sequences along the de novo ribonucleotide biosynthesis pathways are limited. Here we show that all three reactions of pyrimidine nucleobase biosynthesis that convert aspartate to orotate proceed at 60 °C without photochemistry under aqueous conditions in the presence of metals such as Cu(2+) and Mn(4+). Combining reactions into one‐pot variants is also possible. Life may not have invented pyrimidine nucleobase biosynthesis from scratch, but simply refined existing nonenzymatic reaction channels. This work is a first step towards uniting metabolic theories of life's origin with those centered around genetic molecules. John Wiley and Sons Inc. 2022-04-05 2022-06-07 /pmc/articles/PMC9325535/ /pubmed/35304939 http://dx.doi.org/10.1002/anie.202117211 Text en © 2022 The Authors. Angewandte Chemie International Edition published by Wiley-VCH GmbH https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Communications Yi, Jing Kaur, Harpreet Kazöne, Wahnyalo Rauscher, Sophia A. Gravillier, Louis‐Albin Muchowska, Kamila B. Moran, Joseph A Nonenzymatic Analog of Pyrimidine Nucleobase Biosynthesis |
title | A Nonenzymatic Analog of Pyrimidine Nucleobase Biosynthesis |
title_full | A Nonenzymatic Analog of Pyrimidine Nucleobase Biosynthesis |
title_fullStr | A Nonenzymatic Analog of Pyrimidine Nucleobase Biosynthesis |
title_full_unstemmed | A Nonenzymatic Analog of Pyrimidine Nucleobase Biosynthesis |
title_short | A Nonenzymatic Analog of Pyrimidine Nucleobase Biosynthesis |
title_sort | nonenzymatic analog of pyrimidine nucleobase biosynthesis |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9325535/ https://www.ncbi.nlm.nih.gov/pubmed/35304939 http://dx.doi.org/10.1002/anie.202117211 |
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